Incidental Mutation 'R2056:Dscaml1'
ID |
228199 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dscaml1
|
Ensembl Gene |
ENSMUSG00000032087 |
Gene Name |
DS cell adhesion molecule like 1 |
Synonyms |
4921507G06Rik, 4930435C18Rik |
MMRRC Submission |
040061-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.416)
|
Stock # |
R2056 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
9 |
Chromosomal Location |
45338735-45665011 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 45661430 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glycine
at position 1776
(D1776G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000034592
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000034592]
|
AlphaFold |
Q4VA61 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000034592
AA Change: D1776G
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000034592 Gene: ENSMUSG00000032087 AA Change: D1776G
Domain | Start | End | E-Value | Type |
low complexity region
|
3 |
17 |
N/A |
INTRINSIC |
low complexity region
|
28 |
55 |
N/A |
INTRINSIC |
IG_like
|
96 |
168 |
1.22e0 |
SMART |
IG
|
189 |
277 |
1.15e-3 |
SMART |
IGc2
|
296 |
359 |
2.54e-14 |
SMART |
IGc2
|
385 |
451 |
8.12e-13 |
SMART |
IGc2
|
478 |
550 |
9.55e-10 |
SMART |
IGc2
|
575 |
640 |
9.78e-7 |
SMART |
IGc2
|
666 |
734 |
5.93e-6 |
SMART |
IGc2
|
760 |
832 |
6.75e-10 |
SMART |
IG
|
853 |
943 |
1e-3 |
SMART |
FN3
|
945 |
1029 |
6.64e-7 |
SMART |
FN3
|
1045 |
1133 |
9.46e-12 |
SMART |
FN3
|
1148 |
1234 |
3.2e-9 |
SMART |
FN3
|
1249 |
1332 |
3.48e-10 |
SMART |
IGc2
|
1363 |
1428 |
1.49e-11 |
SMART |
FN3
|
1442 |
1522 |
3.42e-9 |
SMART |
FN3
|
1537 |
1618 |
2.14e-1 |
SMART |
low complexity region
|
1671 |
1683 |
N/A |
INTRINSIC |
low complexity region
|
2018 |
2026 |
N/A |
INTRINSIC |
low complexity region
|
2035 |
2069 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000214151
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000215027
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.4%
- 20x: 95.4%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the Ig superfamily of cell adhesion molecules and is involved in neuronal differentiation. The encoded membrane-bound protein localizes to the cell surface, where it forms aggregates that repel neuronal processes of the same cell type. [provided by RefSeq, Sep 2016] PHENOTYPE: Mice homozygous for a gene trapped allele exhibit impaired self-avoidance in multiple cell types in the retina. [provided by MGI curators]
|
Allele List at MGI |
All alleles(4) : Gene trapped(4) |
Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg2 |
T |
C |
6: 58,667,525 (GRCm39) |
V129A |
probably benign |
Het |
Adh1 |
A |
G |
3: 137,992,676 (GRCm39) |
D264G |
probably damaging |
Het |
Ahnak2 |
T |
A |
12: 112,748,626 (GRCm39) |
D407V |
probably benign |
Het |
Alas1 |
T |
C |
9: 106,118,489 (GRCm39) |
E211G |
probably damaging |
Het |
Alkbh1 |
C |
T |
12: 87,490,520 (GRCm39) |
|
probably benign |
Het |
Ankmy1 |
T |
C |
1: 92,809,553 (GRCm39) |
I662V |
possibly damaging |
Het |
Ano1 |
A |
G |
7: 144,201,789 (GRCm39) |
V334A |
probably damaging |
Het |
Apc |
A |
G |
18: 34,449,481 (GRCm39) |
R2092G |
probably damaging |
Het |
Arhgap18 |
C |
T |
10: 26,730,904 (GRCm39) |
T122I |
probably benign |
Het |
Atp2b4 |
G |
T |
1: 133,654,275 (GRCm39) |
Q777K |
probably benign |
Het |
Brap |
G |
A |
5: 121,801,529 (GRCm39) |
G95S |
probably damaging |
Het |
Cbfa2t2 |
G |
A |
2: 154,377,077 (GRCm39) |
A587T |
probably damaging |
Het |
Ccdc180 |
A |
G |
4: 45,932,477 (GRCm39) |
I1308V |
probably benign |
Het |
Ccser1 |
T |
A |
6: 61,399,936 (GRCm39) |
|
probably null |
Het |
Cd84 |
A |
G |
1: 171,700,317 (GRCm39) |
T145A |
possibly damaging |
Het |
Cmtm4 |
A |
C |
8: 105,081,920 (GRCm39) |
F156V |
probably damaging |
Het |
Cntln |
G |
A |
4: 84,967,911 (GRCm39) |
R710K |
probably benign |
Het |
Csn1s1 |
A |
T |
5: 87,819,387 (GRCm39) |
T15S |
possibly damaging |
Het |
Cul9 |
T |
C |
17: 46,854,298 (GRCm39) |
T135A |
probably benign |
Het |
Cyp2d10 |
T |
A |
15: 82,288,015 (GRCm39) |
I363F |
probably damaging |
Het |
Dhx38 |
G |
T |
8: 110,289,352 (GRCm39) |
|
probably benign |
Het |
Dis3 |
A |
T |
14: 99,336,251 (GRCm39) |
I85N |
possibly damaging |
Het |
Dmbt1 |
G |
A |
7: 130,707,900 (GRCm39) |
A1381T |
possibly damaging |
Het |
Erbin |
A |
G |
13: 103,966,824 (GRCm39) |
S1209P |
probably benign |
Het |
Fat4 |
T |
A |
3: 38,945,319 (GRCm39) |
M1404K |
possibly damaging |
Het |
Fbxo45 |
G |
T |
16: 32,057,346 (GRCm39) |
Q183K |
possibly damaging |
Het |
Frmd4b |
C |
T |
6: 97,389,448 (GRCm39) |
|
probably null |
Het |
Fzd7 |
A |
G |
1: 59,523,361 (GRCm39) |
S415G |
probably benign |
Het |
Gpd2 |
T |
A |
2: 57,229,025 (GRCm39) |
|
probably null |
Het |
Gsk3b |
T |
A |
16: 38,008,271 (GRCm39) |
D192E |
probably benign |
Het |
Gstcd |
T |
C |
3: 132,787,814 (GRCm39) |
I295V |
probably benign |
Het |
Gucy1a1 |
A |
G |
3: 82,016,592 (GRCm39) |
L132P |
possibly damaging |
Het |
Il12b |
A |
C |
11: 44,298,727 (GRCm39) |
T61P |
probably damaging |
Het |
Il7 |
A |
T |
3: 7,638,975 (GRCm39) |
N130K |
probably damaging |
Het |
Itih3 |
A |
C |
14: 30,631,481 (GRCm39) |
|
probably null |
Het |
Kdm5b |
T |
A |
1: 134,540,952 (GRCm39) |
D681E |
probably benign |
Het |
Kif11 |
A |
G |
19: 37,390,660 (GRCm39) |
N408D |
probably benign |
Het |
Kng2 |
TATGACCATGACCATGACCATGACCATGACCATGACCAT |
TATGACCATGACCATGACCATGACCATGACCAT |
16: 22,806,703 (GRCm39) |
|
probably benign |
Het |
Kremen2 |
T |
C |
17: 23,961,691 (GRCm39) |
E272G |
possibly damaging |
Het |
Krt9 |
G |
T |
11: 100,082,321 (GRCm39) |
N201K |
probably damaging |
Het |
Lmbr1 |
G |
A |
5: 29,438,092 (GRCm39) |
P304L |
probably benign |
Het |
Lrrfip1 |
A |
G |
1: 91,043,539 (GRCm39) |
N648S |
probably benign |
Het |
Mab21l3 |
C |
A |
3: 101,722,469 (GRCm39) |
V386L |
possibly damaging |
Het |
Mamdc4 |
T |
C |
2: 25,454,180 (GRCm39) |
Q1149R |
probably benign |
Het |
Mast1 |
A |
G |
8: 85,646,995 (GRCm39) |
F677L |
possibly damaging |
Het |
Mcoln3 |
A |
G |
3: 145,833,979 (GRCm39) |
D173G |
probably benign |
Het |
Mmrn1 |
C |
T |
6: 60,921,789 (GRCm39) |
T82I |
probably benign |
Het |
Mtcl2 |
C |
T |
2: 156,864,747 (GRCm39) |
G1154S |
probably benign |
Het |
Muc5ac |
A |
G |
7: 141,345,772 (GRCm39) |
T203A |
probably benign |
Het |
Myo9b |
T |
C |
8: 71,812,334 (GRCm39) |
I2035T |
possibly damaging |
Het |
Ndst3 |
T |
C |
3: 123,465,534 (GRCm39) |
N146S |
probably damaging |
Het |
Neu4 |
A |
G |
1: 93,950,172 (GRCm39) |
T21A |
possibly damaging |
Het |
Nos1ap |
G |
A |
1: 170,155,215 (GRCm39) |
L267F |
probably damaging |
Het |
Or14c40 |
A |
T |
7: 86,313,591 (GRCm39) |
K240N |
probably damaging |
Het |
Or3a4 |
A |
T |
11: 73,944,819 (GRCm39) |
Y255* |
probably null |
Het |
Or4p8 |
A |
G |
2: 88,727,105 (GRCm39) |
F279L |
probably damaging |
Het |
Phc1 |
T |
C |
6: 122,310,299 (GRCm39) |
N136S |
probably damaging |
Het |
Prkdc |
A |
G |
16: 15,545,469 (GRCm39) |
T1862A |
probably benign |
Het |
Psd2 |
A |
G |
18: 36,139,744 (GRCm39) |
D596G |
possibly damaging |
Het |
Psmc3 |
T |
C |
2: 90,888,433 (GRCm39) |
F315L |
probably benign |
Het |
Rerg |
G |
A |
6: 137,034,878 (GRCm39) |
T42I |
probably benign |
Het |
Rif1 |
T |
A |
2: 51,983,588 (GRCm39) |
M577K |
probably damaging |
Het |
Sap30 |
T |
C |
8: 57,940,282 (GRCm39) |
|
probably null |
Het |
Scn2b |
T |
C |
9: 45,036,815 (GRCm39) |
Y108H |
probably damaging |
Het |
Senp2 |
C |
T |
16: 21,832,949 (GRCm39) |
T79I |
probably damaging |
Het |
Serpinb2 |
T |
C |
1: 107,451,543 (GRCm39) |
V232A |
probably damaging |
Het |
Sgpp2 |
T |
A |
1: 78,393,588 (GRCm39) |
L197Q |
probably damaging |
Het |
Slc27a4 |
T |
C |
2: 29,700,953 (GRCm39) |
W320R |
probably damaging |
Het |
Spmip4 |
T |
C |
6: 50,550,725 (GRCm39) |
R575G |
possibly damaging |
Het |
Tgm4 |
T |
C |
9: 122,890,835 (GRCm39) |
I54T |
probably damaging |
Het |
Thbs4 |
T |
A |
13: 92,927,387 (GRCm39) |
D34V |
probably benign |
Het |
Tlcd4 |
T |
G |
3: 121,001,070 (GRCm39) |
I188L |
probably benign |
Het |
Tmem176b |
G |
A |
6: 48,813,267 (GRCm39) |
T64I |
probably damaging |
Het |
Tmod2 |
T |
C |
9: 75,484,524 (GRCm39) |
E248G |
probably benign |
Het |
Ttc6 |
T |
A |
12: 57,784,479 (GRCm39) |
D1849E |
probably benign |
Het |
Ttn |
T |
C |
2: 76,615,882 (GRCm39) |
D8360G |
possibly damaging |
Het |
Unc80 |
A |
G |
1: 66,679,711 (GRCm39) |
E2094G |
possibly damaging |
Het |
Vmn2r18 |
A |
T |
5: 151,508,160 (GRCm39) |
D321E |
probably damaging |
Het |
|
Other mutations in Dscaml1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00418:Dscaml1
|
APN |
9 |
45,581,498 (GRCm39) |
nonsense |
probably null |
|
IGL00497:Dscaml1
|
APN |
9 |
45,663,536 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00895:Dscaml1
|
APN |
9 |
45,662,551 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01011:Dscaml1
|
APN |
9 |
45,594,970 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01086:Dscaml1
|
APN |
9 |
45,613,960 (GRCm39) |
splice site |
probably benign |
|
IGL01125:Dscaml1
|
APN |
9 |
45,660,930 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01132:Dscaml1
|
APN |
9 |
45,663,626 (GRCm39) |
nonsense |
probably null |
|
IGL01356:Dscaml1
|
APN |
9 |
45,658,155 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01459:Dscaml1
|
APN |
9 |
45,653,981 (GRCm39) |
nonsense |
probably null |
|
IGL01552:Dscaml1
|
APN |
9 |
45,359,206 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02033:Dscaml1
|
APN |
9 |
45,595,080 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02044:Dscaml1
|
APN |
9 |
45,658,241 (GRCm39) |
nonsense |
probably null |
|
IGL02095:Dscaml1
|
APN |
9 |
45,359,001 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02166:Dscaml1
|
APN |
9 |
45,594,999 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02262:Dscaml1
|
APN |
9 |
45,643,378 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02262:Dscaml1
|
APN |
9 |
45,656,414 (GRCm39) |
missense |
probably benign |
|
IGL02340:Dscaml1
|
APN |
9 |
45,581,474 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02604:Dscaml1
|
APN |
9 |
45,655,626 (GRCm39) |
unclassified |
probably benign |
|
IGL02619:Dscaml1
|
APN |
9 |
45,359,094 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02805:Dscaml1
|
APN |
9 |
45,359,195 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03409:Dscaml1
|
APN |
9 |
45,581,401 (GRCm39) |
missense |
probably damaging |
1.00 |
D3080:Dscaml1
|
UTSW |
9 |
45,595,623 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03050:Dscaml1
|
UTSW |
9 |
45,654,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R0149:Dscaml1
|
UTSW |
9 |
45,653,978 (GRCm39) |
nonsense |
probably null |
|
R0582:Dscaml1
|
UTSW |
9 |
45,579,562 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0629:Dscaml1
|
UTSW |
9 |
45,632,716 (GRCm39) |
missense |
probably damaging |
0.98 |
R0632:Dscaml1
|
UTSW |
9 |
45,643,432 (GRCm39) |
missense |
probably benign |
0.06 |
R0815:Dscaml1
|
UTSW |
9 |
45,656,372 (GRCm39) |
missense |
probably benign |
0.00 |
R1162:Dscaml1
|
UTSW |
9 |
45,663,647 (GRCm39) |
splice site |
probably benign |
|
R1449:Dscaml1
|
UTSW |
9 |
45,653,521 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1474:Dscaml1
|
UTSW |
9 |
45,596,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R1481:Dscaml1
|
UTSW |
9 |
45,583,941 (GRCm39) |
missense |
probably benign |
0.01 |
R1533:Dscaml1
|
UTSW |
9 |
45,361,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R1542:Dscaml1
|
UTSW |
9 |
45,660,738 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1572:Dscaml1
|
UTSW |
9 |
45,632,631 (GRCm39) |
missense |
probably benign |
0.00 |
R1627:Dscaml1
|
UTSW |
9 |
45,664,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R1634:Dscaml1
|
UTSW |
9 |
45,584,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R1713:Dscaml1
|
UTSW |
9 |
45,663,988 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1777:Dscaml1
|
UTSW |
9 |
45,595,054 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1812:Dscaml1
|
UTSW |
9 |
45,662,584 (GRCm39) |
critical splice donor site |
probably null |
|
R1834:Dscaml1
|
UTSW |
9 |
45,594,930 (GRCm39) |
missense |
probably benign |
0.00 |
R1907:Dscaml1
|
UTSW |
9 |
45,651,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R1953:Dscaml1
|
UTSW |
9 |
45,581,522 (GRCm39) |
missense |
probably benign |
0.01 |
R2193:Dscaml1
|
UTSW |
9 |
45,596,532 (GRCm39) |
missense |
probably benign |
0.21 |
R2497:Dscaml1
|
UTSW |
9 |
45,656,376 (GRCm39) |
missense |
probably benign |
0.00 |
R3768:Dscaml1
|
UTSW |
9 |
45,643,435 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3891:Dscaml1
|
UTSW |
9 |
45,628,782 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4110:Dscaml1
|
UTSW |
9 |
45,643,366 (GRCm39) |
missense |
probably benign |
0.07 |
R4706:Dscaml1
|
UTSW |
9 |
45,361,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R4716:Dscaml1
|
UTSW |
9 |
45,361,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R4719:Dscaml1
|
UTSW |
9 |
45,583,993 (GRCm39) |
missense |
probably benign |
0.13 |
R4770:Dscaml1
|
UTSW |
9 |
45,581,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R4924:Dscaml1
|
UTSW |
9 |
45,656,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R5167:Dscaml1
|
UTSW |
9 |
45,628,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R5346:Dscaml1
|
UTSW |
9 |
45,361,857 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5737:Dscaml1
|
UTSW |
9 |
45,656,483 (GRCm39) |
missense |
probably damaging |
0.99 |
R5977:Dscaml1
|
UTSW |
9 |
45,632,596 (GRCm39) |
missense |
probably benign |
0.19 |
R6073:Dscaml1
|
UTSW |
9 |
45,361,881 (GRCm39) |
missense |
probably benign |
0.22 |
R6276:Dscaml1
|
UTSW |
9 |
45,579,458 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6415:Dscaml1
|
UTSW |
9 |
45,594,975 (GRCm39) |
nonsense |
probably null |
|
R6527:Dscaml1
|
UTSW |
9 |
45,623,482 (GRCm39) |
nonsense |
probably null |
|
R6582:Dscaml1
|
UTSW |
9 |
45,664,104 (GRCm39) |
missense |
probably benign |
0.00 |
R6655:Dscaml1
|
UTSW |
9 |
45,658,235 (GRCm39) |
missense |
probably benign |
0.00 |
R6772:Dscaml1
|
UTSW |
9 |
45,621,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R6799:Dscaml1
|
UTSW |
9 |
45,361,881 (GRCm39) |
missense |
probably benign |
0.22 |
R6892:Dscaml1
|
UTSW |
9 |
45,595,128 (GRCm39) |
missense |
probably damaging |
0.99 |
R6918:Dscaml1
|
UTSW |
9 |
45,341,805 (GRCm39) |
missense |
probably benign |
|
R6967:Dscaml1
|
UTSW |
9 |
45,585,821 (GRCm39) |
missense |
probably damaging |
0.97 |
R7214:Dscaml1
|
UTSW |
9 |
45,581,437 (GRCm39) |
missense |
probably benign |
0.01 |
R7286:Dscaml1
|
UTSW |
9 |
45,654,044 (GRCm39) |
critical splice donor site |
probably null |
|
R7315:Dscaml1
|
UTSW |
9 |
45,656,423 (GRCm39) |
missense |
probably benign |
0.00 |
R7338:Dscaml1
|
UTSW |
9 |
45,585,802 (GRCm39) |
missense |
probably benign |
0.12 |
R7343:Dscaml1
|
UTSW |
9 |
45,664,214 (GRCm39) |
missense |
probably benign |
|
R7395:Dscaml1
|
UTSW |
9 |
45,613,703 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7439:Dscaml1
|
UTSW |
9 |
45,621,624 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7484:Dscaml1
|
UTSW |
9 |
45,660,744 (GRCm39) |
splice site |
probably null |
|
R7545:Dscaml1
|
UTSW |
9 |
45,596,681 (GRCm39) |
missense |
probably benign |
0.11 |
R7979:Dscaml1
|
UTSW |
9 |
45,595,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R8005:Dscaml1
|
UTSW |
9 |
45,628,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R8181:Dscaml1
|
UTSW |
9 |
45,658,140 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8262:Dscaml1
|
UTSW |
9 |
45,658,438 (GRCm39) |
intron |
probably benign |
|
R8428:Dscaml1
|
UTSW |
9 |
45,653,884 (GRCm39) |
missense |
probably benign |
0.00 |
R8725:Dscaml1
|
UTSW |
9 |
45,341,759 (GRCm39) |
missense |
probably benign |
0.00 |
R8727:Dscaml1
|
UTSW |
9 |
45,341,759 (GRCm39) |
missense |
probably benign |
0.00 |
R8796:Dscaml1
|
UTSW |
9 |
45,359,026 (GRCm39) |
missense |
probably damaging |
0.99 |
R8840:Dscaml1
|
UTSW |
9 |
45,634,718 (GRCm39) |
missense |
probably damaging |
0.99 |
R9291:Dscaml1
|
UTSW |
9 |
45,359,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R9394:Dscaml1
|
UTSW |
9 |
45,661,354 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9610:Dscaml1
|
UTSW |
9 |
45,579,522 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9611:Dscaml1
|
UTSW |
9 |
45,579,522 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9653:Dscaml1
|
UTSW |
9 |
45,643,466 (GRCm39) |
critical splice donor site |
probably null |
|
R9699:Dscaml1
|
UTSW |
9 |
45,654,315 (GRCm39) |
missense |
probably damaging |
0.97 |
X0058:Dscaml1
|
UTSW |
9 |
45,663,426 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Dscaml1
|
UTSW |
9 |
45,584,089 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Predicted Primers |
PCR Primer
(F):5'- TCAGCACTGGATGAAGACATAC -3'
(R):5'- TGTGGTCAAGGTCTCCAGAC -3'
Sequencing Primer
(F):5'- CATACACAAATTTGAGGAGGACATC -3'
(R):5'- ACTGGAGCTCATCAATTTGGC -3'
|
Posted On |
2014-09-17 |